Device Recall Kwires and Guide Wres 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Amendia, Inc 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    75858
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0881-2017
  • 사례 시작날짜
    2016-11-22
  • 사례 상황
    Open, Classified
  • 사례 국가
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Pin, fixation, smooth - Product Code HTY
  • 원인
    The rods are packaged in packages with unacceptable seals. in some cases, the integrity of the seal is compromised by channels or voids.
  • 조치
    Amendia sent an Urgent Medical Device Recall letter dated November 22, 2016, to all affected customers. The letter requested that customers examine their inventory and quarantine the product. The letter also requested that they contact Amendia to confirm receipt of the letter and to obtain a Return Material Authorization for any product on hand. Customers with questions were instructed to call the following numbers: 770-575-5224 770-575-5236 770-575-5369 For questions regarding this recall call 404-610-7215.

Device

  • 모델명 / 제조번호(시리얼번호)
    Part Number 9080-12U Lot Number 121306, 121307, 122628, 122721, 124400, 132732, 135403; Part Number 9080-18T Lot Number 122486, 122626, 123957, 124408, 127435, 129132, 129803, 129935, 131072, 135560, 135566, 135567; Part Number 9080-18U Lot Number 122470, 123948, 129802, 129936, 130390, 130391, 131073; Part Number 9080-24T Lot Number 133359; Part Number 9080-24U Lot Number 134108, 134112, 134908; Part Number 9080B-18T Lot Number 124547, 126820, 127437, 131454, 132592, 134181, 135401; Part Number 9080B-18U Lot Number 122468, 123938, 126504, 127436, 129800, 130947, 131453, 132750, 133645, 134169, 134907, 135563, 135578, 135579, 135580; Part Number 9080B-24U Lot Number 122239, 130392, 130393, 131839, 133988, 135359, 135360, 135400; Part Number 9080B-N-18T Lot Number 124137, 125331, 128472, 130612, 132229, 135584, 135585, 137464; Part Number 9080B-N-18U Lot Number 123556, 125199, 126821, 128348, 128469, 129443, 129915, 130836, 131626, 133118, 134180, 135208; Part Number 9080L-18U Lot Number 127877, 128351, 130389, 130946, 133261, 135210, 135593; Part Number 9080-N-18T Lot Number 122488, 123863, 130914; Part Number 9080-N-18U Lot Number 122487, 123564, 124402, 126125, 129005, 129077, 133499, 135562, 137462.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    Nationwide Distribution to AL, AZ, AR, CA, CO, FL, GA, IA, KS, KY, LA, MA, MI, MN, MO, NV, NJ, NC, SC, TN, TX, VA, WA, WV, WI and Puerto Rico
  • 제품 설명
    K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U; K-Wire Threaded 1.4mm x 18, Part Number 9080-18T; K-Wire Non-Threaded 1.4mm x 18, Part Number 9080-18U; 1.4mm x 24 Threaded Guide Wire, Part Number 9080-24T; K-Wire Non-Threaded 24, Part Number 9080-24U; Blunt K-Wire, 18 inches, Threaded, Part Number 9080B-18T; Blunt K-Wire, 18 inches, Unthreaded, Part Number 9080B-18U; Blunt K-Wire, 24 inches, Unthreaded, Part Number 9080B-24U; 1.4mm x 18 Blunt Threaded Nitinol Guide Wire, Part Number 9080B-N-18T; 1.4mm x 18" Blunt Non-Threaded Nitinol Guide Wire, Part Number 9080B-N-18U; Lodestar K-wire Non-Threaded, 18, Part Number 9080L-18U; 1.4mm x 18 Threaded Nitinol Guide Wire, Part Number 9080-N-18T; 1.4mm x 18 Non-Threaded Nitinol Guide Wire, Part Number 9080-N-18U || The guide wire is passed through the cannulated handle of the Dual Stylet Needles and pressed into the bone
  • Manufacturer

Manufacturer

  • 제조사 주소
    Amendia, Inc, 1755 W Oak Pkwy, Marietta GA 30062-2260
  • 제조사 모회사 (2017)
  • Source
    USFDA